LINC01560
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Summary
LINC01560 (long intergenic non-protein coding RNA 1560, HGNC:27333) is a long non-coding RNA gene on chromosome Xp11.3.
At a glance
- Gene type: non-coding (lncRNA) — no protein product; not a drug target. Variant/disease associations are omitted (they would be positional, from an overlapping protein-coding gene).
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:27333 |
| Approved symbol | LINC01560 |
| Name | long intergenic non-protein coding RNA 1560 |
| Location | Xp11.3 |
| Locus type | RNA, long non-coding |
| Status | Approved |
| Ensembl gene | ENSG00000196741 |
| Ensembl biotype | lncRNA |
| Entrez | 203414 |
| RNAcentral | URS00007E3FA4 — lncRNA, 2528 nt, 1 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 lncRNA
ENST00000357412
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000357412 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001421084 | 47483571 | 47484823 |
Expression profiles
Bgee: expression breadth ubiquitous, 207 present calls, max score 89.94.
FANTOM5 (CAGE): breadth ubiquitous, TPM avg 1.9451 / max 32.0460, expressed in 1185 samples.
FANTOM5 promoters (2 alternative TSS)
| Promoter ID | TPM avg | Samples expressed |
|---|---|---|
| 196203 | 1.7406 | 1093 |
| 196204 | 0.2044 | 76 |
Top tissues by expression
239 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| buccal mucosa cell | CL:0002336 | 89.94 | gold quality |
| primordial germ cell in gonad | CL:0000670 ∩ UBERON:0000991 | 83.83 | gold quality |
| ganglionic eminence | UBERON:0004023 | 82.08 | gold quality |
| ileal mucosa | UBERON:0000331 | 81.65 | gold quality |
| ventricular zone | UBERON:0003053 | 78.77 | gold quality |
| cortical plate | UBERON:0005343 | 77.82 | gold quality |
| gastrocnemius | UBERON:0001388 | 76.92 | gold quality |
| muscle of leg | UBERON:0001383 | 76.89 | gold quality |
| tibialis anterior | UBERON:0001385 | 75.35 | silver quality |
| monocyte | CL:0000576 | 75.25 | gold quality |
| leukocyte | CL:0000738 | 74.88 | gold quality |
| rectum | UBERON:0001052 | 73.46 | gold quality |
| body of uterus | UBERON:0009853 | 73.23 | gold quality |
| smooth muscle tissue | UBERON:0001135 | 72.60 | gold quality |
| islet of Langerhans | UBERON:0000006 | 72.52 | gold quality |
| cerebellar hemisphere | UBERON:0002245 | 72.42 | gold quality |
| hindlimb stylopod muscle | UBERON:0004252 | 72.41 | gold quality |
| cerebellar cortex | UBERON:0002129 | 72.30 | gold quality |
| mucosa of transverse colon | UBERON:0004991 | 72.25 | gold quality |
| endocervix | UBERON:0000458 | 71.98 | gold quality |
| right hemisphere of cerebellum | UBERON:0014890 | 71.62 | gold quality |
| cerebellum | UBERON:0002037 | 71.56 | gold quality |
| left ovary | UBERON:0002119 | 71.54 | gold quality |
| descending thoracic aorta | UBERON:0002345 | 71.11 | gold quality |
| secondary oocyte | CL:0000655 | 70.70 | gold quality |
| ectocervix | UBERON:0012249 | 70.67 | gold quality |
| popliteal artery | UBERON:0002250 | 70.64 | gold quality |
| tibial artery | UBERON:0007610 | 70.64 | gold quality |
| ovary | UBERON:0000992 | 70.52 | gold quality |
| aorta | UBERON:0000947 | 70.27 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 1.32 |
Regulation
Is transcription factor: no
Cross-species orthologs
0 orthologs
Protein
Non-coding RNA — no protein product; not a drug target.
Function
No curated pathway, Gene-Ontology, or interaction data.
Disease & clinical
No curated disease, variant, or cancer-driver associations.
Drugs & pharmacology
No drug or pharmacology data — not an established drug target.
Related Atlas pages
- Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): epilepsy, X-linked 1, with variable learning disabilities and behavior disorders, thrombocytopenia 1, Wiskott-Aldrich syndrome, X-linked severe congenital neutropenia